During mitosis the clathrin binds directly to the microtubules or microtubule-associated proteins.

Other molecules that can be degraded by calpains are microtubule subunits, microtubule-associated proteins, and neurofilaments.

Assembly, disassembly, and catastrophe rates depend on which microtubule-associated proteins (MAPs) are present.

Microtubule-bound arrestins recruit certain proteins to the cytoskeleton, which affects their activity and/or redirects it to microtubule-associated proteins.

Microtubule-associated proteins (MAPs) associate with microtubules at the midzone and the spindle poles to regulate their dynamics.

While tubulin monomers and microtubule-associated proteins (MAPs) are present, organized microtubules are not present.

In cell biology, microtubule-associated proteins (MAPs) are proteins that interact with the microtubules of the cellular cytoskeleton.

Excessively active calpain breaks down molecules in the cytoskeleton such as spectrin, microtubule subunits, microtubule-associated proteins, and neurofilaments.

CLASP1 belongs to a family of microtubule-associated proteins involved in attachment of microtubules to the cell cortex in animals and plants.

Orchestration refers to the hypothetical process by which connective proteins, known as microtubule-associated proteins (MAPs) influence or orchestrate the quantum processing of the microtubules.

They regulate polarity in neuronal cell models and appear to function redundantly in phosphorylating microtubule-associated proteins and in regulating microtubule stability.

MAP1A and MAP1B are microtubule-associated proteins which mediate the physical interactions between microtubules and components of the cytoskeleton.

It is also dependent on several microtubule-associated proteins such as EB1 and Adenomatous Polyposis Coli (APC).

Microtubule-associated proteins 1A/1B light chain 3A is a protein that in humans is encoded by the MAP1LC3A gene.

In the last decade, some researchers who are sympathetic to Penrose's ideas have proposed an alternative scheme for quantum processing in microtubules based on the interaction of tubulin tails with microtubule-associated proteins, motor proteins and presynaptic scaffold proteins.

The severing of microtubules by katanin is regulated by nucleotide exchange factors, which can exchange ADP with ATP, protective microtubule-associated proteins (MAPs), and the p80 subunit (p60 severs microtubules much better in the presence of p80).

Purification of tubulin from pig brain Phosphocellulose-purified tubulin (PC-tubulin) free of microtubule-associated proteins (MAPs) was obtained by warm/cold polymerization/depolymerization with the addition of a final phosphocellulose chromatography step to separate tubulin from MAPs [ 37 38 ] .

Like most microtubule-associated proteins, tau is normally regulated by phosphorylation; however, in AD patients, hyperphosphorylated tau accumulates as paired helical filaments that in turn aggregate into masses inside nerve cell bodies known as neurofibrillary tangles and as dystrophic neurites associated with amyloid plaques.